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Quantification method of ctDNA using cell-free DNA methylation profile for noninvasive screening and monitoring of colon cancer

Authors :
Hyojung Ryu
Ji-Hoon Kim
Yeo Jin Kim
Hahyeon Jeon
Byoung-Chul Kim
Yeonsu Jeon
Yeonkyung Kim
Hyebin Bak
Younghui Kang
Changjae Kim
Hyojin Um
Ji-Hye Ahn
Hwi Hyun
Byung Chul Kim
Inho Song
Sungwon Jeon
Jong Bhak
Eon Chul Han
Source :
Clinical Epigenetics, Vol 16, Iss 1, Pp 1-11 (2024)
Publication Year :
2024
Publisher :
BMC, 2024.

Abstract

Abstract Background Colon cancer ranks as the second most lethal form of cancer globally. In recent years, there has been active investigation into using the methylation profile of circulating tumor DNA (ctDNA), derived from blood, as a promising indicator for diagnosing and monitoring colon cancer. Results We propose a liquid biopsy-based epigenetic method developed by utilizing 49 patients and 260 healthy controls methylation profile data to screen and monitor colon cancer. Our method initially identified 901 colon cancer-specific hypermethylated (CaSH) regions in the tissues of the 49 cancer patients. We then used these CaSH regions to accurately quantify the amount of circulating tumor DNA (ctDNA) in the blood samples of these same patients, utilizing cell-free DNA methylation profiles. Notably, the methylation profiles of ctDNA in the blood exhibited high sensitivity (82%) and specificity (93%) in distinguishing patients with colon cancer from the control group, with an area under the curve of 0.903. Furthermore, we confirm that our method for ctDNA quantification is effective for monitoring cancer patients and can serve as a valuable tool for postoperative prognosis. Conclusions This study demonstrated a successful application of the quantification of ctDNA among cfDNA using the original cancer tissue-derived CaSH region for screening and monitoring colon cancer.

Details

Language :
English
ISSN :
18687083
Volume :
16
Issue :
1
Database :
Directory of Open Access Journals
Journal :
Clinical Epigenetics
Publication Type :
Academic Journal
Accession number :
edsdoj.20c621c5ea84b5b91fa811429ad0999
Document Type :
article
Full Text :
https://doi.org/10.1186/s13148-024-01708-9